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Holandric heredity
Holandric inheritance
Holandric transmission
SLRL test
Sex-conditioned character
Sex-influenced character
Sex-linked character
Sex-linked disease
Sex-linked gene
Sex-linked gene
Sex-linked hereditary disease
Sex-linked heredity
Sex-linked inheritance
Sex-linked recessive inheritance
Sex-linked recessive lethal assay
Sex-linked recessive lethal test
X-linked gene
X-linked inheritance
Y-linked inheritance

Translation of "sex-linked inheritance " (English → French) :

sex-linked inheritance | sex-linked heredity | X-linked inheritance

hérédité liée au sexe | hérédité gonosomique
biologie > génétique
biologie > génétique


sex-linked recessive inheritance

transmission récessive liée au sexe
biologie > génétique
biologie > génétique


sex-linked recessive lethal assay | sex-linked recessive lethal test | SLRL test

épreuve de létalité récessive liée au sexe | épreuve du gène létal récessif lié au sexe | épreuve SLRL | test de létalité récessive liée au sexe | test SLRL
IATE - Health
IATE - Health


sex-conditioned character | sex-influenced character | sex-linked character

caractère lié au sexe
IATE - Health
IATE - Health


sex-linked hereditary disease (1) | sex-linked disease (2)

maladie héréditaire liée au sexe
Automation | Medicine & biology
Médecine (Automatisation) | Pathologie (Sciences médicales et biologiques) | Biologie (Sciences médicales et biologiques)


holandric inheritance | Y-linked inheritance | holandric heredity | holandric transmission

hérédité holandrique | transmission holandrique
biologie > génétique
biologie > génétique


sex-linked gene | X-linked gene

gène lié au sexe
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences


A rare X-linked inherited type of ocular albinism described in one African kindred (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately

albinisme oculaire avec surdité sensorielle tardive
SNOMEDCT-BE (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately / 722054007
SNOMEDCT-BE (disorder) / 722054007


Sex-linked gene (function)

gène lié au sexe
SNOMEDCT-CA (function) / 35416005
SNOMEDCT-CA (substance) / 35416005


A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)

maladie de Charcot-Marie-Tooth liée à l'X type 4
SNOMEDCT-BE (in particular of the peroneal group) / 763400005
SNOMEDCT-BE (disorder) / 763400005




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'sex-linked inheritance'

Date index:2023-09-21 -

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